6 results
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16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
AGILTRAC .035 PERIPHERAL DILATATION CATHETER
FDA Adverse Event
Malfunction
·GUIDANT ENDOVASCULAR SOLUTIONS·Product code LIT·May 2, 2006
OMNILINK .035 STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code FGE·May 8, 2009
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
AGILTRAC .035 PERIPHERAL DILATATION CATHETER
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code LIT·February 2, 2009
SYRINGE 50ML CT
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 23, 2021
CURAPLEX
FDA Adverse Event
Malfunction
·BOUND TREE MEDICAL, LLC·Product code BTM·December 21, 2023